Canonical Allele Identifier: CA516732293

Gene: NONO

Linked Data

• gnomAD v4: X-71299977-T-C
• MyVariant Identifiers: chrX:g.70519827T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.71299977T>C , CM000685.2:g.71299977T>C	GRCh38
NC_000023.10:g.70519827T>C , CM000685.1:g.70519827T>C	GRCh37
NC_000023.9:g.70436552T>C	NCBI36
NG_046742.1:g.21786T>C
NG_054891.1:g.3703T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276079.13:c.1317T>C MANE Select	ENSP00000276079.8:p.Ala439=
ENST00000373856.8:c.1415T>C	ENSP00000362963.4:p.Leu472Pro
ENST00000420903.6:c.1317T>C	ENSP00000410299.2:p.Ala439=
ENST00000450092.6:c.1317T>C	ENSP00000415777.2:p.Ala439=
ENST00000454976.2:c.1317T>C	ENSP00000406673.2:p.Ala439=
ENST00000473525.2:n.2025T>C
ENST00000676495.1:n.2728T>C
ENST00000676499.1:n.2273T>C
ENST00000676797.1:c.1050T>C	ENSP00000503920.1:p.Ala350=
ENST00000677014.1:c.*1144T>C	ENSP00000503813.1:n.*1144T>C
ENST00000677218.1:n.2488T>C
ENST00000677245.1:c.*1526T>C	ENSP00000503929.1:n.*1526T>C
ENST00000677274.1:c.1317T>C	ENSP00000504314.1:p.Ala439=
ENST00000677446.1:c.1317T>C	ENSP00000503031.1:p.Ala439=
ENST00000677612.1:c.1317T>C	ENSP00000504351.1:p.Ala439=
ENST00000677766.1:n.3722T>C
ENST00000677826.1:n.2059T>C
ENST00000677879.1:c.1137T>C	ENSP00000504090.1:p.Ala379=
ENST00000677977.1:n.3149T>C
ENST00000678231.1:c.1317T>C	ENSP00000503233.1:p.Ala439=
ENST00000678323.1:n.2415T>C
ENST00000678335.1:c.*230T>C	ENSP00000503769.1:n.*230T>C
ENST00000678437.1:c.1308T>C	ENSP00000504007.1:p.Ala436=
ENST00000678660.1:c.1332T>C	ENSP00000504665.1:p.Ala444=
ENST00000678830.1:c.1407T>C	ENSP00000504263.1:p.Ala469=
ENST00000679029.1:c.*131T>C	ENSP00000504193.1:n.*131T>C
ENST00000679267.1:n.3524T>C
ENST00000276079.12:c.1317T>C	ENSP00000276079.8:p.Ala439=
ENST00000373841.5:c.1317T>C	ENSP00000362947.1:p.Ala439=
ENST00000373856.7:c.1317T>C	ENSP00000362963.3:p.Ala439=
ENST00000472185.1:n.61-542T>C
ENST00000473525.1:n.1091T>C
ENST00000474431.5:n.352T>C
ENST00000490044.5:n.2024T>C
ENST00000535149.5:c.1050T>C	ENSP00000441364.1:p.Ala350=
NM_001145408.1:c.1317T>C	NP_001138880.1:p.Ala439=
NM_001145409.1:c.1317T>C	NP_001138881.1:p.Ala439=
NM_001145410.1:c.1050T>C	NP_001138882.1:p.Ala350=
NM_007363.4:c.1317T>C	NP_031389.3:p.Ala439=
NM_007363.5:c.1317T>C MANE Select	NP_031389.3:p.Ala439=
NM_001145408.2:c.1317T>C	NP_001138880.1:p.Ala439=
NM_001145409.2:c.1317T>C	NP_001138881.1:p.Ala439=
NM_001145410.2:c.1050T>C	NP_001138882.1:p.Ala350=